A New Radio Dial

"Democrats and Republicans in Congress have struck a deal on a bill they say will help keep children and teens safe online. The KIDS Act could pass on the House floor as soon as next week; if enacted, it would fundamentally change the way everyone — not just kids — accesses the internet.

At stake is your ability to use many social media platforms without revealing your identity. 

That’s because the KIDS Act at least strongly incentivizes — and, for some services, outright requires — age verification. Many platforms will turn to age verification to avoid potential liability under the law. Companies like X, video-sharing services like Vimeo, and others with a history of users’ populating social feeds with edgy content may be required to verify users’ ages because they host a certain amount of content deemed “sexual material harmful to minors,” a term that the KIDS Act defines broadly. 

That’s a big problem for people who need to be able to use the internet anonymously, since, as Taylor Lorenz has previously written about in The Intercept, “there’s no way to reliably verify someone’s age without verifying who they are.” 

Threats to online anonymity harm everyone, but one group is often overlooked: journalists and the sources who talk to them. Age verification requirements will help the Trump administration carry out its vendetta against the press by creating new avenues to identify journalists’ confidential sources. [...]

I'm so tired

I would like help buying food! I'm a black transman who does art full time! So I'd appreciate it if you could help me get food! I pay for all my own food and groceries on my own and pay rent as well while doing art full time!!

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KOSA IS MOVING FORWARD IN THE HOUSE!

It's part of a package called the KIDS Act, filled with digital ID and age verification and censorship!

MAKE THOSE PHONES RING!! CALL YOUR HOUSE REPRESENTATIVES ALL WEEK

202-224-3121 i HIGHLY encourage everyone to read the bills in the KIDS Act, because you will be doing more than 95% of people who read and introduce these bills

Discovered last year I couldn’t look at my 2015 MacBook Air without it triggering nausea and migraines, and figured the screen died. Have been getting by on my phone, but concluded I really need a laptop again.

Saved up, realised I could afford a brand new MacBook Neo, and got one.

-And I couldn’t spend more than five minutes looking at the screen without massive eye strain, nausea, vertigo, and if I pushed it, I-need-to-lie-down-in-a-dark-room-for-hours migraines.

Looking up MacBook and Eyestrain explained what is going on. The liquid retina displays that Apple currently has uses Pulse Width Modulation or PWM. In order to give the screens a deeper depth of colour and contrast, PWM flickers between several hundred to thousand times a second.

And there is currently no way to turn it off. There are settings and apps to reduce it, but there is no way to stop the screen from flickering. Checked Apple forums, called Apple Support, and the time I could look at the screen kept shrinking. Got the laptop Tuesday, returned it Friday, today is Sunday and I’m still dealing with a vertigo migraine.

For MacBooks, it seems to vary on the computer model and the software it uses. In retrospect, the issue with my MacBook Air started after a major software update.

And it’s not just an Apple thing. Current Windows and Android screens do the same thing. There’s even a Reddit for people who are sensitive to PWM flickers to help find computers and screens that won’t trigger eyestrain and headaches.

So, yeah. This week has been a learning experience. But for those who are prone to headaches and migraines, this may be something to be aware of, cause I was not.

Navigating gender dysphoria? Be heard and be counted in the science.

These people are forming this "study"

I wonder what else they've done?

huh. well she's just leading the survey, maybe the other two are better?

nope, all bad people who only want to hurt us.

I had to pay off the last of my late cat's vet bill this month. was going to put a hundred towards it, but they asked for all of it. which is whatever, it's over and I don't have to worry about it anymore. but I am on a fixed income, so between rent, household necessities, and the vet bill I basically zeroed out my account by the fifth. my food stamps were also cut, which isn't great. my wheelchair broke today too, which is. not great. the part that held the back wheels on to the rest of the chair was made out of fucking plastic for some reason, and the hook snapped in half. I don't have any way to fix it. the company it came from isn't well known for sending replacement parts, either. the last two times I was forced to ask them for help, I got 'we'll send it once we get spare parts in!' over and over every time I messaged them, up to the point where I just gave up after a month solid of daily messages.

so I have like $30 in food stamps for the rest of the month, and a $20 in my wallet I am saving for quarters to do laundry. I can probably manage to skid by with a bit of discomfort this month, considering I have been careful with the money I have spent on food, but I would rather not deal with that if I don't HAVE to. I don't know what to do about the wheelchair, but at least I can get food to make the rest of this month a little less painful with a little help. if you got a couple bucks you're willing to throw my way, I'd appreciate it a lot. it's not, like, desperate at the moment? it's mostly to keep me from having to live off of the spare ramen and plain pasta I've picked up a stupid amount of for basically this exact purpose.

Any little donation will help. Please, she’s my baby and she’s in pain.

Reblog appreciated.

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There are 760,000 Australians on the National Disability Insurance Scheme, the system that - if they feel like it and your personalised plan says you get to have it - provides funding for everything from personal hygiene care to support workers to therapies to assistive technology. It's already very hard for disabled people to get on the NDIS, regardless of your disability. It's near impossible to access most support and equipment without being on the NDIS. And the government has announced that they want that number to drop to 600,000 in four years. 160,000 of us cut off the Scheme - and countless more denied access. This will cause deaths. People will die and people will suffer because there is no safety net. The NDIS is the only option for most of us. Even private health insurance doesn't cover most of these things. Nobody will swoop in to save us.

The bill wants to give the (non disabled!) NDIS minister basically unlimited power to cut our funding. They're already planning what they'd do with that power. What rights they'll strip from us. What dignity and freedom they'll remove to make their budget look better.

The bill wants to force people to try every treatment out there before they're allowed to be on the NDIS. Including if the treatment is literally impossible to access. There’s a lot of us living in regional areas or out bush who can't just pop to the capital cities for specialists. This will especially hurt disabled First Nations people in regional and remote communities, who already experience limited access to healthcare. Oh, and it includes chemical restraint, too. The government has directly refused to exclude chemical restraint from the required process, calling it "trialling medication".

If you're australian and worried, the ABC did a good breakdown of the proposed changes.

I know australia stuff doesn't really pop up on the radar on this site, but I want everyone to know what's going on. What we're fighting for here. Your australian disabled friends might be NDIS participants fearing for their life, rights, and freedom. They might not be a participant and afraid these changes mean they never will have access. We deserve better. The government built a system with no backup plan, and now they want hundreds of thousands of disabled people to pay the price for their bad planning.

- Nobody needs to apologise for venting in the notes or reblogs. We're scared and upset and deserve to be heard.

What to do:

- australians: don't give up! There's still people fighting this, it's not law yet. And even if it passes we can fight them on it. Most disabled peoples' organisations are fighting this, so organisations like People With Disability Australia and area specific groups. Membership to most of them is free if you're disabled. PWDA sends out a list of the news about us each week to keep us informed.

🔗Disabled People Against Cuts are leading a charge. There's always a way to make politicians pay attention even if we have to park our arses on their front step. Share support and resources where you can and keep an eye on the others in your community if you're able to. Talk to local support clinics about Coles and Woolworths vouchers for those facing a lot of uncertainty. And get your flu shot if you're able. Nobody needs the next protest to give everyone the flu.

- non-australians: keep watching. You might also benefit from seeing what DPAC are doing and if they ever call for international support. Supporting the disabled australians you know and refusing to be kept in the dark about what’s being done to marginalised people internationally is good preparation for lots of ways to help, it means you're ready to go if something you can help with appears and don't lose time educating yourself. Many of the situations with the NDIS have deliberately had short time frames to act, to try and stop us from having a voice.

context from the notes:

- When I said health insurance doesn't cover disability supports, I don't mean "it's very expensive so people can't access it". I mean the services often won't take on anyone who doesn't have an NDIS plan. Even then, it's common for services to prefer people who are "plan managed" or "agency managed", meaning someone else handles our invoices, because they feel "self managed" people might not pay them fast enough.

- People have been getting "check in" phone calls from the agency. It’s secretly plan reviews for them to reduce people's funding. If they call you and you don’t have your support people with you, they are lying when they say you don't need them. Tell them to organise a time to call later so you can have your support people. This kind of warning is the only reason I knew to contact my support coordinator when I got this phone call. Others I have seen didn't know and got their plan cut. And it takes years to try and change a plan or appeal it through the tribunal.

- Someone in the notes has identified herself as a support coordinator and offered to help with questions for people concerned about their plan via DMs (thank you @andromedusia). This is very kind of her and I also hope mentioning this here doesn't cause you any trouble, very sorry if it does.

- Also, not thrilled to find out they might be phasing out support coordinators. Lots of us are dependent on them - a support coordinator is someone who helps us understand out plan and connect with supports, and often helps with advocacy too. They’ll save money on us purely because we won't know where to go or what the plans mean. They use a lot of confusing terms in the plans. I'd be screwed without my support coordinator.

- Oh they also want to use a standardised assessment tool to tell how disabled we are, after a decade of having to pay out of pocket for specialists who know us to provide reports. This is actually worse because the tool doesn’t have to be done by a qualified professional and doesn’t work on people with a lot of different disabilities. The government is very good at somehow turning "bad" into "worse".

- Yeah. 760,000 australians is actually not that many. There's 27 million people living here. 85% of disabled australians aren't on the NDIS. Now, a lot of disabled people don't necessarily need the kind of support the NDIS provides, but you know who I don't trust to make that decision? The government who doesn't want to pay for it.

- None of this fixes the existing problems with access for First Nations people or people from culturally and linguistically diverse backgrounds. I'm pretty sure a standardised assessment tool will actually only make that way worse. No room for professionals to work with cultural sensitivity and humility to understand the impact of someone's disability, or the varying ways First Nations communities may construct and talk about disability that don't necessarily align with the settler government's convenient definition. Just checkboxes.

- This isn't even our "conservative" government party in power. This is the centre/centre-left party, Labor. The 'Liberal party' (note: not liberal) would likely do worse. But I don't think there's much to be grateful for when this will kill people. And probably won't stop later conservative cuts anyway. Because we cost too much.

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